HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394636Generated: October 29, 2026
2-Bromoethanol → 12-(2-bromo-ethoxy)-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cyclooctene
https://huagongshe.com/reaction/394636
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 12-bromo-2,10-dichloro-12H-5,7-dioxadibenzo[a,d]cyclooctene | HCID 22727778 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 12-(2-bromo-ethoxy)-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cyclooctene | HCID 22727880 | 82.4% |
Reaction Steps
A mixture of 12-bromo-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cyclooctene (900 mg, 2.5 mmol), 2-bromoethanol (3.75 g, 30 mmol) and potassium carbonate (1.0 g, 7.2 mmol) in dichloromethane (10 mL) was heated at 120° C. for 4 h. The reaction mixture was concentrated in vacuo, added water (25 mL) and the product extracted with ethyl acetate (3×25 mL). The combined organic phases were dried (MgSO4), filtered and evaporated to give 832 mg (82%) of 12-(2-bromo-ethoxy)-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cyclooctene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06602901B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-bbb40de2dfc5410e9e5c478503ee3737 |
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| Source note | uspto-grants-2003_08 |
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